Search results for "Quinoline"

showing 10 items of 391 documents

CCDC 1054356: Experimental Crystal Structure Determination

2016

Related Article: Nicolas Sok, Maria Nikolantonaki, Stephane Guyot, Thanh Dat Nguyen, Anne-Sophie Viaux, Franck Bagala, Yoann Rousselin, Florence Husson, Régis Gougeon, Rémi Saurel|2017|Sens.Actuators,B|242|865|doi:10.1016/j.snb.2016.09.171

Space GroupCrystallographybis(4-((13-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)amino)-4-oxobut-2-enoic acid) 2-(isopropylideneamino)-1H-benzo[de]isoquinoline-13(2H)-dione acetone solvate monohydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1506160: Experimental Crystal Structure Determination

2017

Related Article: Nicole Parra, Julio B. Belmar, Claudio A. Jiménez, Jorge Pasán, Catalina Ruiz-Pérez|2017|CrystEngComm|19|1076|doi:10.1039/C6CE02393B

Space GroupCrystallographycatena-[bis(mu-N-(4-((isoquinolin-1-ylcarbonyl)amino)butyl)isoquinoline-1-carboxamide)-di-silver(i) bis(perchlorate) methanol solvate dihydrate]Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 709725: Experimental Crystal Structure Determination

2009

Related Article: I.S.Jahro, D.Onggo, Ismunandar, S.I.Rahayu, M.C.Munoz, A.B.Gaspar, M.Seredyuk, P.Gutlich, J.A.Real|2008|Inorg.Chim.Acta|361|4047|doi:10.1016/j.ica.2008.03.122

Space GroupCrystallographyclambdacdelta-tris(2-(2-Pyridyl)quinoline)-iron(ii) bis(tetrafluoroborate) ethanol solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 709727: Experimental Crystal Structure Determination

2009

Related Article: I.S.Jahro, D.Onggo, Ismunandar, S.I.Rahayu, M.C.Munoz, A.B.Gaspar, M.Seredyuk, P.Gutlich, J.A.Real|2008|Inorg.Chim.Acta|361|4047|doi:10.1016/j.ica.2008.03.122

Space GroupCrystallographyclambdacdelta-tris(2-(2-Pyridyl)quinoline)-iron(ii) bis(tetrafluoroborate) ethanol solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 644919: Experimental Crystal Structure Determination

2008

Related Article: F.Durola, L.Russo, J.-P.Sauvage, K.Rissanen, O.S.Wenger|2007|Chem.-Eur.J.|13|8749|doi:10.1002/chem.200700684

Space GroupCrystallographytris(88'-bis(4'-Methoxybiphenyl-4-yl)-33'-biisoquinoline-NN')-iron(ii) bis(hexachloroantimonate) nitrobenzene unknown solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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N-Heterocyclic choline analogues based on 1,2,3,4-tetrahydro(iso)quinoline scaffold with anticancer and anti-infective dual action

2016

Pharmacological effects of biologically active “small molecules” can be improved by their targeted modification, which affects drug delivery and interaction with tumor cells and microorganisms. We aimed to evaluate anticancer and antimicrobial activity of lipid-like choline derivatives modified via simultaneous introduction of tetrahydro(iso)quinoline based pharmacophore system at nitrogen atom and long chain alkyl substituent at oxygen atom. Target compounds were synthesized under phase-transfer catalysis conditions followed by quaternization, and evaluated for cytotoxicity and NO-generation ability on HT-1080 and MG-22A tumor cell lines and NIH 3T3 normal mouse fibroblasts, and screened f…

StereochemistryAntineoplastic AgentsMicrobial Sensitivity TestsGram-Positive Bacteriamedicine.disease_cause01 natural sciencesDNA gyraseCholineInhibitory Concentration 50Mice03 medical and health scienceschemistry.chemical_compoundDrug Delivery Systems0302 clinical medicineAnti-Infective AgentsCell Line TumorNeoplasmsGram-Negative BacteriamedicineAnimalsHumansCytotoxicityEscherichia coliPharmacologybiology010405 organic chemistryQuinolineFungiBiological activityGeneral MedicineAntimicrobialbiology.organism_classificationProteus mirabilis0104 chemical scienceschemistry030220 oncology & carcinogenesisNIH 3T3 CellsQuinolinesAntibacterial activityPharmacological Reports
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Beyond Pseudo‐natural Products: Sequential Ugi/Pictet‐Spengler Reactions Leading to Steroidal Pyrazinoisoquinolines That Trigger Caspase‐Independent …

2021

In this work, we describe how stereochemically complex polycyclic compounds can be generated by applying a synthetic sequence comprising an intramolecular Ugi reaction followed by a Pictet-Spengler cyclization on steroid-derived scaffolds. The resulting compounds, which combine a fragment derived from a natural product and a scaffold not found in nature. are both structurally distinct and globally similar to natural products at the same time, and interrogate an alternative region of the chemical space. One of the new compounds showed significant antiproliferative activity on HepG2 cells through a caspase-independent cell-death mechanism, an appealing feature when new antitumor compounds are…

StereochemistryAntineoplastic AgentsSequence (biology)01 natural sciencesBiochemistryPiperazineschemistry.chemical_compoundDrug DiscoveryHumansGeneral Pharmacology Toxicology and PharmaceuticsCell ProliferationPharmacologyBiological ProductsNatural productPictet–Spengler reactionCell DeathMolecular Structure010405 organic chemistryOrganic ChemistryCaspase independentStereoisomerismHep G2 CellsIsoquinolinesChemical space0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryCaspasesIntramolecular forceHepg2 cellsMolecular MedicineUgi reactionSteroidsDrug Screening Assays AntitumorChemMedChem
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Regioselective substitution of 6,7-dichloroquinoline-5,8-dione: synthesis and X-ray crystal structure of 4a,10,11-triazabenzo[3,2-a]fluorene-5,6-dion…

2003

6,7-Dichloroquinoline-5,8-dione (1) was reacted with a number of 2-aminopyridine derivatives. Of the several possible products of this reaction, 4a,10,11-triazabenzo[3,2-a]fluorene-5,6-dione (6), produced by condensation and rearrangement, was obtained as the major product, and its structure was subsequently unambigously determined by X-ray crystallographic study. Ortho-quinones were produced via nucleophilic substitution at position C7, which was unexpected, considering that para-quinones were produced via C6 substitution in the reaction between compound 1 and ethyl acetoacetate in our previous work. Such unexpected nucleophilic substitution at C7 provides an effective, yet simple route, t…

StereochemistryClinical BiochemistryPharmaceutical ScienceAntineoplastic AgentsCrystallography X-RayBiochemistryMedicinal chemistryChemical synthesisInhibitory Concentration 50chemistry.chemical_compoundNucleophilic aromatic substitutionDrug DiscoveryTumor Cells CulturedNucleophilic substitutionHumansMolecular BiologySubstitution reactionFluorenesMolecular StructureOrganic ChemistryQuinonesRegioselectivityStereoisomerismQuinonechemistryDoxorubicinEthyl acetoacetateQuinolinesMolecular MedicineAcid hydrolysisDrug Screening Assays AntitumorBioorganic & Medicinal Chemistry
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3,4-Dihydroxy- and 3,4-methylenedioxy- phenanthrene-type alkaloids with high selectivity for D2 dopamine receptor.

2013

Abstract Dopamine-mediated neurotransmission plays an important role in relevant psychiatric and neurological disorders. Nowadays, there is an enormous interest in the development of new drugs acting at the dopamine receptors (DR) as potential new targets for the treatment of schizophrenia or Parkinson’s disease. Previous studies have revealed that isoquinoline compounds such as tetrahydroisoquinolines (THIQs) can behave as selective D 2 dopaminergic alkaloids. In the present study we have synthesized five aporphine compounds and five phenanthrene alkaloids and evaluated their potential dopaminergic activity. Binding studies on rat striatal membranes were used to evaluate their affinity and…

StereochemistryClinical BiochemistryPharmaceutical ScienceNeurotransmissionPharmacologyBiochemistryMethylenedioxychemistry.chemical_compoundAlkaloidsDrug DiscoveryAnimalsHumansAporphineIsoquinolineMolecular BiologyChemistryReceptors Dopamine D2Organic ChemistryDopaminergicParkinson DiseasePhenanthrenePhenanthrenesCorpus StriatumRatsDopamine receptorSchizophreniaMolecular MedicineSelectivityBioorganicmedicinal chemistry letters
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Synthesis and cytotoxicity of 6,11-Dihydro-pyrido- and 6,11-Dihydro-benzo[2,3-b]phenazine-6,11-dione derivatives

2003

6,11-Dihydro-pyrido[2,3-b]phenazine-6,11-diones and 6,11-dihydro-benzo[2,3-b]phenazine-6,11-diones were synthesized from 6,7-dichloro-5,8-quinolinedione and 2,3-dichloro-1,4-naphthoquinone. The study on the cytotoxicity on these products revealed that the pyridophenazinediones, tetracyclic heteroquinone analogues with three nitrogen atoms exhibited a high cytotoxicity on several human tumor cell lines. Compound 9c and 9e showed in vitro antitumor activity comparable or superior to doxorubicin against the human ovarian tumor cells (SK-OV-3) and the human CNS cells (XF 498). The IC(50) value for compound 9e was 0.06 microM against the human CNS cells (XF 498), which was 2.6 times higher than …

StereochemistryClinical BiochemistryPhenazinePharmaceutical ScienceAntineoplastic AgentsCrystallography X-RayBiochemistryChemical synthesisInhibitory Concentration 50Structure-Activity Relationshipchemistry.chemical_compoundDrug DiscoveryTumor Cells CulturedNucleophilic substitutionHumansStructure–activity relationshipCytotoxicityMolecular BiologyMolecular StructureOrganic ChemistryIn vitroQuinonechemistryDoxorubicinCell cultureQuinolinesPhenazinesMolecular MedicineDrug Screening Assays AntitumorNaphthoquinonesBioorganic & Medicinal Chemistry
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